Isonipecotic acid

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Fswitzer4 (talk | contribs) at 02:03, 21 June 2020 (Added FDA UNII). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Isonipecotic acid
Skeletal formula of isonipecotic acid
Skeletal formula of isonipecotic acid
Ball-and-stick model
Ball-and-stick model
Names
IUPAC name
4-Piperidinecarboxylic acid
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.007.158 Edit this at Wikidata
EC Number
  • 207-872-3
UNII
  • InChI=1S/C6H11NO2/c8-6(9)5-1-3-7-4-2-5/h5,7H,1-4H2,(H,8,9) ☒N
    Key: SRJOCJYGOFTFLH-UHFFFAOYSA-N ☒N
  • InChI=1/C6H11NO2/c8-6(9)5-1-3-7-4-2-5/h5,7H,1-4H2,(H,8,9)
    Key: SRJOCJYGOFTFLH-UHFFFAOYAD
  • C1CNCCC1C(=O)O
Properties
C6H11NO2
Molar mass 129.16 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Isonipecotic acid is a heterocyclic compound which acts as a GABAA receptor partial agonist.[1]

It consists of a piperidine ring with a carboxylic acid moiety in the iso position (and as such is also known as "4-piperidinecarboxylic acid").

References

  1. ^ Mortensen M, Kristiansen U, Ebert B, Frølund B, Krogsgaard-Larsen P, Smart TG (June 2004). "Activation of single heteromeric GABA(A) receptor ion channels by full and partial agonists". The Journal of Physiology. 557 (Pt 2): 389–413. doi:10.1113/jphysiol.2003.054734. PMC 1665090. PMID 14990676.


Stub icon

This sedative-related article is a stub. You can help Wikipedia by expanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Isonipecotic_acid&oldid=963661049"